Cited by 773Retinoids in leukemia and cellular processesPeroxisome Proliferator-Activated ReceptorsGenomics and Chromatin Dynamics

Nuclear retinoid receptors and the transcription of retinoid-target genes

Bastien, Julie, Rochette-Egly, Cécile·2004·Gene

Abstract

The pleiotropic effects of retinoids are mediated by nuclear retinoid receptors (RARs and RXRs) which are ligand-activated transcription factors. In response to retinoid binding, RAR/RXR heterodimers undergo major conformational changes and orchestrate the transcription of specific gene networks, through binding to specific DNA response elements and recruiting cofactor complexes that act to modify local chromatin structure and/or engage the basal transcription machinery. Then the degradation of RARs and RXRs by the ubiquitin-proteasome controls the magnitude and the duration of the retinoid response. RARs and RXRs also integrate a variety of signaling pathways through phosphorylation events which cooperate with the ligand for the control of retinoid-target genes transcription. These different modes of regulation reveal unexpected levels of complexity in the dynamics of retinoid-dependent transcription.

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Crossref · 10.1016/j.gene.2003.12.005

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  • Classically, RAREs are composed of two direct repeats (DR) of a core hexameric motif (A/G)G(G/T)TCA separated by 1, 2, or 5 nucleotides and referred as DR1, DR2, and DR5.

    “Classically, RAREs are composed of two direct repeats (DR) of a core hexameric motif (A/G) G (G/T) TCA separated by 1, 2, or 5 nucleotides and referred as DR1, DR2, and DR5 ( 26, 76, 77 ) ( Fig. 3B ).”
  • RARs heterodimerized with RXRs bind to specific retinoic acid response elements (RARE) located in the promoters of target genes.

    “RARs heterodimerized with RXRs bind to specifi c retinoic acid response elements (RARE) located in the promoters of target genes.”

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Authors
Bastien, J., & Rochette-Egly, C.
Affiliations
Centre National de la Recherche Scientifique (FR)
Venue
Gene
Publisher
Elsevier BV
Published
2004-03
Volume
328
Pages
1-16
ISSN
0378-1119 (ISSN-L)
OpenAlex
W2133197725
Cited by
773
References
15
Citations by year
2026: 13 · 2025: 17 · 2024: 22 · 2023: 28 · 2022: 14 · 2021: 22 · 2020: 24 · 2019: 22 · 2018: 21 · 2017: 32 · 2016: 28 · 2015: 36 · 2014: 40 · 2013: 46 · 2012: 42
FWCI
4.40
Type
journal article
Language
en
Open access
closed
Locations
  • Gene (publishedVersion)
  • PubMed (publishedVersion)
  • HAL (submittedVersion)
Funders
  • Association pour la Recherche sur le Cancer
  • Institut National de la Santé et de la Recherche Médicale
  • Ligue Contre le Cancer
  • Centre National de la Recherche Scientifique
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Retinoids in leukemia and cellular processes
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Peroxisome Proliferator-Activated Receptors
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
Keywords
retinoic acid receptor, retinoid X receptor, ligand-activated transcription factors, receptor heterodimers, DNA response elements, chromatin remodeling, ubiquitin-proteasome degradation, receptor phosphorylation, signaling pathway integration
MeSH terms
Animals, Base Sequence, Binding Sites, Cysteine Endopeptidases, Gene Expression Regulation, Humans, Models, Genetic, Multienzyme Complexes, Phosphorylation, Retinoids, Transcription, Genetic, Receptors, Retinoic Acid, Ubiquitin, Proteasome Endopeptidase Complex

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